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loading...| Preferred Name |
Reye syndrome |
| ID |
http://www.orpha.net/ORDO/Orphanet_3096 |
| definition |
A rare, systemic disease characterized by persistent vomiting with confusion, lethargy, disorientation, hyperreflexia, hyperventilation, and tachycardia, with rapid progression to seizures, non-inflammatory encephalopathy, coma and death. It typically develops between 12 hours and 3 weeks after recovery from a viral illness, such as upper respiratory tract infection or gastroenteritis. Hepatomegaly, acute hepatic steatosis, fatty liver degeneration and multiple laboratory abnormalities are associated. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3096 |
| hasDbXref |
ICD-10:G93.7 ICD-11:8E46 MeSH:D012202 MedDRA:10039012 UMLS:C0035400 |
| label |
Reye syndrome |
| notation |
ORPHA:3096 |
| part_of | |
| prefixIRI |
ORDO:Orphanet_3096 |
| prefLabel |
Reye syndrome |
| treeView | |
| subClassOf |
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